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首页> 外文期刊>Analytical chemistry >Determination of zeta-Potential and Tortuosity in Rat Organotypic Hippocampal Cultures from Electroosmotic Velocity Measurements under Feedback Control
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Determination of zeta-Potential and Tortuosity in Rat Organotypic Hippocampal Cultures from Electroosmotic Velocity Measurements under Feedback Control

机译:在反馈控制下通过电渗速度测量确定大鼠器官型海马培养物中的ζ电势和曲折度

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Extracellular translational motion in the brain is generally considered to be governed by diffusion and tortuosity. However, the brain as a whole has a significant zeta-potential, thus translational motion is also governed by electrokinetic effects under a naturally occurring or applied electric field. We have previously measured zeta-potential and tortuosity in intact brain tissue; however, the method was tedious. In this work, we use a four-electrode potentiostat to control the potential difference between two microreference electrodes in the tissue, creating a constant electric field. Additionally, some alterations have been made to simplify our previous procedure. The method entails simultaneously injecting two 70 kDa dextran conjugated fluorophores into rat organotypic hippocampal cultures and observing their mobility using fluorescence microscopy. We further present two methods of data analysis: regression and two-probe analysis. Statistical comparisons are made between the previous and current methods as well as between the two data analysis methods. In comparison to the previous method, the current, simpler method with data analysis by regression gives statistically indistinguishable mean values of zeta-potential and tortuosity, with a similar variability for zeta-potential, -21.3 +- 2.8 mV, and a larger variability for the tortuosity, 1.98 +- 0.12. On the other hand, we find that the current method combined with the two-probe analysis produces accurate and more precise results, with a zeta-potential of -22.8 +- 0.8 mV and a tortuosity of 2.24 +- 0.10.
机译:通常认为大脑中的细胞外平移运动受扩散和曲折度支配。但是,大脑整体具有显着的ζ电势,因此平移运动也受自然产生或施加的电场下的电动势控制。我们之前已经测量了完整大脑组织中的ζ电位和曲折度;但是,该方法很繁琐。在这项工作中,我们使用四电极恒电位仪来控制组织中两个微参比电极之间的电势差,从而产生恒定的电场。此外,已进行一些更改以简化我们以前的过程。该方法需要同时向大鼠器官型海马培养物中注射两个70 kDa右旋糖酐偶联的荧光团,并使用荧光显微镜观察其活动性。我们进一步介绍了两种数据分析方法:回归分析和双探针分析。在先前方法和当前方法之间以及两种数据分析方法之间进行统计比较。与以前的方法相比,当前的更简单方法是通过回归进行数据分析,得出zeta势和曲折率的统计平均值无法区分,zeta势的相似性变化为-21.3 +-2.8 mV,而zeta势的变化性更大曲折度1.98±-0.12。另一方面,我们发现当前的方法与双探针分析相结合可产生准确且更精确的结果,ζ电位为-22.8 +-0.8 mV,曲折度为2.24 +-0.10。

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